Ered. Assessments of SAS, pain intensity, mean arterial pressure and heart rate were made every

Ered. Assessments of SAS, pain intensity, mean arterial pressure and heart rate were made every 20 min for the first 6 hours after starting the opioid infusion and then hourly. Results: See Table. Conclusions: The dosing algorithm allowed effective provision of optimal sedation with remifentanil without the addition of propofol in the majority of patients. The similarity of the results for fentanyl probably reflects the stringent conditions of the dosing algorithm,Table Remifentanil (n = 77) Mean modified ICU admission SAPS II score Duration of assessment of optimal sedation (hours; mean, range) hours of optimal sedation (mean, SD) Number ( ) of patients requiring propofol Fentanyl (n = 75)28.2 13.7 (3?3)27.7 14.2 (< 1?3)88.3 (14.1) 27 (35 )89.3 (15.1) 30 (40 )which demanded frequent monitoring and adjustment of the level of sedation to ensure that a SAS score of 4 was maintained. The remifentanil regimen was well tolerated and the safety profile was similar to fentanyl. The titratability and predictable duration of action make remifentanil a very effective opioid for the provision of analgesia/sedation in ICU patients. This study (USA30206) was supported by a grant from Glaxo Wellcome.P200 An investigation of the offset of pharmacodynamic effects of remifentanil following prolonged infusion in ICU patients withvarying degrees of renal dysfunction: preliminary resultsA Wilmer, A Bodenham, D Breen, V Bach, J Bonde, P Kessler, S Albrecht, S Shaikh UZ Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium Introduction: Remifentanil HCl (R) is a mu-opioid agonist with a rapid onset ( 1 min) and offset of action (t1/2 < 10 min) due to its organ-independent metabolism by non-specific tissue and blood esterases. These properties make it readily titratable and even afterSCritical CareVol 5 Suppl21st International Symposium on Intensive Care and Emergency Medicineprolonged infusion the effects of R do not accumulate. EXEL04286652 pubmed ID:http://www.ncbi.nlm.nih.gov/pubmed/20718733 Its major metabolite, remifentanil acid (RA) is eliminated by the kidneys and its elimination is prolonged as a result of increasing renal dysfunction. However RA has been reported to have 1/4600 mu-opioid potency of the parent compound. This study assessed the offset of pharmacodynamic (PD) effects of R in ICU patients with varying degrees of renal dysfunction receiving R for provision of sedation and analgesia. Methods: R (starting rate 6? /kg/h) was administered as a continuous infusion for up to 72 hours in 40 ICU patients (10 normal/mild renal impairment, creatinine clearance 50 ml/min: 30 moderate/severe renal impairment, creatinine clearance < 50 ml/min) who required sedation and analgesia. At scheduled times (8, 24, 48 and 72 hours) R was down titrated until the offset of PD effects (eg changes in sedation, pain intensity, respiratory function or haemodynamic variables) were seen. On confirmation of the offset of PD effects, R was continued at the original rate. Results: See Table. Conclusions: The offset of the PD effects of R were consistent and independent of the duration of infusion even in patients with aP201 Phenobarbital: a good choice for long-term sedationTable Renal status: normal/mild PD offset (min) (mean, SD) 15.6 ?7.4 (n = 10) 13.8 ?7.7 (n = 10) 16.1 ?7.2 (n = 8) 14.8 ?5.7 (n = 6) Renal status: moderate/severe PD offset (min) (mean, SD) 19 ?15.7 (n = 27) 20.3 ?11.7 (n = 20) 15.4 ?7.4 (n = 12) 25.3 ?12.6 (n = 11)Time of down titration (h) 8 24 48significant degree of renal dysfunction. R was well tolerated in th.